INTRODUCTIONHeyde Syndrome is a rare condition characterized by a classical triad of Aortic Stenosis, Angiodysplasia of the Gastrointestinal tract often manifesting as Gastrointestinal bleeding and acquired Von Willebrand factor deficiency1,2. Although described by Edward Heyde in 1958, the exact pathophysiology and prevalence are still not clear. This condition is thought to be underreported due to a lack of clinical suspicion and the absence of diagnostic modalities in countries with less equipped health infrastructures. It is more commonly diagnosed at ages over 65 years. Although definite protocols for the management of Heyde Syndrome have not been defined, it has been observed that correction of Aortic Stenosis, with medical and endoscopic interventions for angiodysplasias provides a favorable result3.
